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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 395628Generated: October 25, 2026

1,2,3,4-Tetrahydro-2-naphthalenol → 4-(4-Chlorophenyl)-2-(2-methyl-1-imidazolyl)-5-[3-(5,6,7,8-tetrahydro-2-naphthoxy)propyl]oxazole

https://huagongshe.com/reaction/395628

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2,3,4-Tetrahydro-2-naphthalenolHCID 10747—
ReactantTributylphosphineHCID 13831—
Reactant1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
Reactant4-(4-Chlorophenyl)-2-(2-methyl-1-imidazolyl)-5-oxazolepropanolHCID 9926997—
SolventTetrahydrofuranHCID 8028—
Product4-(4-Chlorophenyl)-2-(2-methyl-1-imidazolyl)-5-[3-(5,6,7,8-tetrahydro-2-naphthoxy)propyl]oxazoleHCID 18174744—

Reaction Steps

To a mixture of 4-(4-chlorophenyl)-2-(2-methyl-1-imidazolyl)-5-oxazolepropanol (318 mg), 2-hydroxytetralin (296 mg), tributylphosphine (405 mg) and tetrahydrofuran (10 ml) was added 1,1′-(azodicarbonyl)dipiperidine (400 mg) at room temperature, and the resulting mixture was stirred for 1 hour. After the reaction mixture was concentrated, the residue was subjected to silica gel column chromatography, and 4-(4-chlorophenyl)-2-(2-methyl-1-imidazolyl)-5-[3-(5,6,7,8-tetrahydro-2-naphthoxy)propyl]oxazole was obtained as an oil from an ethyl acetate-hexane (1:1, v/v)-eluted fraction. (358 mg, 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06605629B1
Source datasetuspto-grants-2003_08
ORD IDord-46c3a4ff77254cdb89118a2a89bc17fe
Source noteuspto-grants-2003_08